HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936584Generated: November 3, 2026
5-Aminobenzimidazole → HCID 178507337, compound
https://huagongshe.com/reaction/1936584
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Aminobenzimidazole | HCID 13623 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178507337 | HCID 178507337 | — |
Reaction Steps
To a solution of 1.08 g of 5-aminobenzimidazole in 20 mL of glacial acetic acid are added 2.68 g of sodium acetate. To this solution is added dropwise 0.4 mL of bromine. The resulting brown precipitate is stirred at room temperature for 2 hours. The reaction mixture is rotary evaporated and the residue is diluted with water and ethyl acetate. The mixture is basified with 1 N sodium hydroxide and decanted. The organic layer is washed with water followed by brine. The aqueous layers are extracted with ethyl acetate; the combined organic layers are dried over magnesium sulfate, filtered and rotary evaporated. The residue is purified by flash column chromatography on silica gel, eluting with 12.5 to 16.5% methanol/methylene chloride followed by recrystallization from hexanes/ethyl acetate to provide 887 mg of 5-amino-4-bromobenzimidazole as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06391878B2 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-322ad2c7a534470ea03ee0c5fe81abf3 |
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| Source note | uspto-grants-2002_05 |
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